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TALEN-mediated editing of the mouse Y chromosome.TALEN 介导的小鼠 Y 染色体编辑。
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2
High-efficiency and heritable gene targeting in mouse by transcription activator-like effector nucleases.转录激活因子样效应物核酸酶在小鼠中实现高效且可遗传的基因靶向。
Nucleic Acids Res. 2013 Jun;41(11):e120. doi: 10.1093/nar/gkt258. Epub 2013 Apr 28.
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The CRISPR system--keeping zebrafish gene targeting fresh.CRISPR 系统——让斑马鱼基因靶向技术保持新鲜。
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Nat Biotechnol. 2013 Jan;31(1):23-4. doi: 10.1038/nbt.2477.
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Highly efficient and specific genome editing in silkworm using custom TALENs.利用定制 TALEN 实现家蚕的高效和特异性基因组编辑。
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TAL Effector-Nucleotide Targeter (TALE-NT) 2.0: tools for TAL effector design and target prediction.TAL 效应物-核苷酸靶向器(TALE-NT)2.0:TAL 效应物设计和靶标预测工具。
Nucleic Acids Res. 2012 Jul;40(Web Server issue):W117-22. doi: 10.1093/nar/gks608. Epub 2012 Jun 12.
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FLASH assembly of TALENs for high-throughput genome editing.TALEN 的 FLASH 组装用于高通量基因组编辑。
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10
Heritable targeted inactivation of myostatin gene in yellow catfish (Pelteobagrus fulvidraco) using engineered zinc finger nucleases.利用工程化锌指核酸酶在黄颡鱼(Pelteobagrus fulvidraco)中实现肌肉生长抑制素基因的可遗传靶向敲除。
PLoS One. 2011;6(12):e28897. doi: 10.1371/journal.pone.0028897. Epub 2011 Dec 14.

利用转录激活样效应因子核酸酶生成肌肉生长抑制素B基因敲除的黄颡鱼(黄颡鱼)

Generation of myostatin B knockout yellow catfish (Tachysurus fulvidraco) using transcription activator-like effector nucleases.

作者信息

Dong Zhangji, Ge Jiachun, Xu Zhiqiang, Dong Xiaohua, Cao Shasha, Pan Jianlin, Zhao Qingshun

机构信息

1 MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center, Nanjing University , Nanjing, China .

出版信息

Zebrafish. 2014 Jun;11(3):265-74. doi: 10.1089/zeb.2014.0974. Epub 2014 May 9.

DOI:10.1089/zeb.2014.0974
PMID:24813227
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4050710/
Abstract

Myostatin (Mstn), a member of the transforming growth factor β superfamily, plays an inhibiting role in mammalian muscle growth. Mammals like human, cattle, mouse, sheep, and dog carrying null alleles of Mstn display a double-muscle phenotype. Mstn is conserved in fish; however, little is known whether the fish with mutated mstn display a similar phenotype to mammals because of the lack of mutant fish with mstn null alleles. Previously, we knocked out one of the duplicated copies of myostatin gene (mstna) in yellow catfish using zinc-finger nucleases. In this study, we report the identification of the second myostatin gene (mstnb) and knockout of mstnb in yellow catfish. The gene comprises three exons. It is predicted to encode 373 amino acid residues. The predicted protein exhibits 59.3% identity with yellow catfish Mstna and 57.3% identity with human MSTN. Employing TALEN (transcription activator-like effector nucleases) technology, we obtained two founders (from four randomly selected founders) of yellow catfish carrying the mutated mstnb gene in their germ cells. Totally, six mutated alleles of mstnb were obtained from the founders. Among the six alleles, four are nonframeshift and two are frameshift mutation. The frameshift mutated alleles include mstnb(nju22), an 8 bp deletion, and mstnb(nju24), a complex type of mutation comprising a 7 bp deletion and a 12 bp insertion. They are predicted to encode function null Mstnb. Our results will help to understand the roles of mstn genes in fish growth.

摘要

肌肉生长抑制素(Mstn)是转化生长因子β超家族的成员之一,在哺乳动物肌肉生长中起抑制作用。携带Mstn无效等位基因的人类、牛、小鼠、绵羊和狗等哺乳动物表现出双肌表型。Mstn在鱼类中是保守的;然而,由于缺乏具有mstn无效等位基因的突变鱼,尚不清楚mstn突变的鱼是否表现出与哺乳动物相似的表型。此前,我们使用锌指核酸酶敲除了黄颡鱼中肌肉生长抑制素基因(mstna)的一个重复拷贝。在本研究中,我们报告了黄颡鱼中第二个肌肉生长抑制素基因(mstnb)的鉴定以及mstnb的敲除。该基因由三个外显子组成。预计它编码373个氨基酸残基。预测的蛋白质与黄颡鱼Mstna的同一性为59.3%,与人类MSTN的同一性为57.3%。利用转录激活样效应核酸酶(TALEN)技术,我们获得了两条在生殖细胞中携带突变mstnb基因的黄颡鱼奠基鱼(从随机选择的四条奠基鱼中获得)。总共从这些奠基鱼中获得了六个mstnb的突变等位基因。在这六个等位基因中,四个是非移码突变,两个是移码突变。移码突变等位基因包括mstnb(nju22),一个8 bp的缺失,以及mstnb(nju24),一种复杂类型的突变,包括一个7 bp的缺失和一个12 bp的插入。预计它们编码无功能的Mstnb。我们的结果将有助于了解mstn基因在鱼类生长中的作用。